Evidence map›Paper›PMID 33920464›Full record

ArticleInternational journal of molecular sciences2021

Role of Electrostatic Interactions in Calcitonin Prefibrillar Oligomer-Induced Amyloid Neurotoxicity and Protective Effect of Neuraminidase.

Ida Cariati, Roberto Bonanni, Mario Marini, Anna Maria Rinaldi, Beatrice Zarrilli, Virginia Tancredi, Claudio Frank, Giovanna D'Arcangelo, Marco Diociaiuti

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Neuraminidase inhibition improves endothelial function in diabetic mice.American journal of physiology. Heart and circulatory physiology · 2023
    Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Ida CariatiMedical-Surgical Biotechnologies and Translational Medicine (Phd), Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.ORCID 0000-0002-2102-5034
Roberto BonanniDepartment of Systems Medicine, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.ORCID 0000-0002-7174-0714
Mario MariniDepartment of Systems Medicine, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.
Anna Maria RinaldiDepartment of Systems Medicine, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.
Beatrice ZarrilliDepartment of Systems Medicine, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.
Virginia TancrediDepartment of Systems Medicine, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.ORCID 0000-0003-4779-2212
Claudio FrankUniCamillus-Saint Camillus International University of Health Sciences, Via di Sant'Alessandro 8, 00131 Rome, Italy.
Giovanna D'ArcangeloDepartment of Systems Medicine, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.ORCID 0000-0002-2105-0395
Marco DiociaiutiCentro Nazionale Malattie Rare, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0002-0749-2824
University of Rome Tor Vergata · ITIstituto Superiore di Sanità · ITSaint Camillus International University of Health and Medical Sciences · IT

Funding

This work was supported by the Italian "Ministero della Salute" with the "Progetto Ordinario di Ricerca Finalizzata (RF-2013-02355682)" RF-2013-02355682
6 · The paper itself

Abstract

Salmon calcitonin is a good model for studying amyloid behavior and neurotoxicity. Its slow aggregation rate allows the purification of low molecular weight prefibrillar oligomers, which are the most toxic species. It has been proposed that these species may cause amyloid pore formation in neuronal membranes through contact with negatively charged sialic acid residues of the ganglioside GM1. In particular, it has been proposed that an electrostatic interaction may be responsible for the initial contact between prefibrillar oligomers and GM1 contained in lipid rafts. Based on this evidence, the aim of our work was to investigate whether the neurotoxic action induced by calcitonin prefibrillar oligomers could be counteracted by treatment with neuraminidase, an enzyme that removes sialic acid residues from gangliosides. Therefore, we studied cell viability in HT22 cell lines and evaluated the effects on synaptic transmission and long-term potentiation by in vitro extracellular recordings in mouse hippocampal slices. Our results showed that treatment with neuraminidase alters the surface charges of lipid rafts, preventing interaction between the calcitonin prefibrillar oligomers and GM1, and suggesting that the enzyme, depending on the concentration used, may have a partial or total protective action in terms of cell survival and modulation of synaptic transmission.

Indexed as

Amyloid NeuropathiesSalmonAnimalsCalcitoninFish ProteinsG(M1) GangliosideMaleMembrane MicrodomainsMiceMice, Inbred BALB CNeuraminidaseStatic ElectricityCalcitoninFish ProteinsG(M1) GangliosideNeuraminidaseamyloid neurotoxicitycell viabilityGM1lipid raftsneuraminidaseneurodegenerationsalmon calcitoninsoluble prefibrillar oligomerssynaptic transmission

Identifiers

PMID33920464
PMCPMC8070249
OpenAlexW3152787947

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.